Incidental Mutation 'IGL01622:Actl11'
ID 278636
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Actl11
Ensembl Gene ENSMUSG00000066368
Gene Name actin-like 11
Synonyms 4921517D21Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01622
Quality Score
Status
Chromosome 9
Chromosomal Location 107805668-107809660 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 107805775 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 33 (S33P)
Ref Sequence ENSEMBL: ENSMUSP00000082150 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085073]
AlphaFold Q9D5V1
Predicted Effect probably benign
Transcript: ENSMUST00000085073
AA Change: S33P

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000082150
Gene: ENSMUSG00000066368
AA Change: S33P

DomainStartEndE-ValueType
low complexity region 223 239 N/A INTRINSIC
low complexity region 301 309 N/A INTRINSIC
low complexity region 374 391 N/A INTRINSIC
low complexity region 492 507 N/A INTRINSIC
low complexity region 697 710 N/A INTRINSIC
ACTIN 858 1207 4.26e-81 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930596D02Rik G A 14: 35,532,024 (GRCm39) Q184* probably null Het
A1bg A C 15: 60,789,742 (GRCm39) I502S possibly damaging Het
Aftph G T 11: 20,659,632 (GRCm39) D730E probably damaging Het
Arhgap29 A G 3: 121,767,773 (GRCm39) probably benign Het
Brf1 T G 12: 112,924,795 (GRCm39) E643A probably benign Het
Caskin1 G T 17: 24,722,914 (GRCm39) probably null Het
Ccnjl T C 11: 43,476,154 (GRCm39) V259A probably benign Het
Ccser2 G T 14: 36,662,920 (GRCm39) T88K probably benign Het
Cdk17 T C 10: 93,074,824 (GRCm39) probably benign Het
Clec16a G A 16: 10,395,774 (GRCm39) S309N possibly damaging Het
Cpxm1 C A 2: 130,233,191 (GRCm39) A633S probably benign Het
Ctnnbl1 A T 2: 157,661,468 (GRCm39) N326I probably damaging Het
Cyp46a1 T C 12: 108,318,234 (GRCm39) V215A possibly damaging Het
Daxx A G 17: 34,132,454 (GRCm39) D528G probably benign Het
Dnah6 T C 6: 73,121,701 (GRCm39) Y1427C probably damaging Het
Dpy19l3 G A 7: 35,422,169 (GRCm39) T228I probably damaging Het
Fam131c C T 4: 141,109,761 (GRCm39) A131V possibly damaging Het
Fat1 A G 8: 45,482,592 (GRCm39) T3061A possibly damaging Het
Fgl2 T A 5: 21,578,175 (GRCm39) L154H possibly damaging Het
Fhod3 T A 18: 25,155,924 (GRCm39) I514K probably benign Het
Ficd G A 5: 113,876,622 (GRCm39) G266S probably damaging Het
Frem3 A G 8: 81,340,544 (GRCm39) T946A probably benign Het
Gan T A 8: 117,913,917 (GRCm39) V105D probably damaging Het
Garin5b A G 7: 4,761,722 (GRCm39) V330A probably benign Het
Gramd1c A G 16: 43,811,061 (GRCm39) V221A probably damaging Het
Hacd1 A G 2: 14,040,667 (GRCm39) V196A probably benign Het
Kcna6 C A 6: 126,715,576 (GRCm39) V438L probably damaging Het
Kif14 T C 1: 136,425,094 (GRCm39) probably benign Het
Klhl41 T C 2: 69,508,582 (GRCm39) V512A probably benign Het
Lrfn1 A G 7: 28,166,111 (GRCm39) T502A probably damaging Het
Notch3 A T 17: 32,377,844 (GRCm39) F105I possibly damaging Het
Or4b13 T G 2: 90,082,953 (GRCm39) K126N probably damaging Het
Or5m10 A T 2: 85,717,306 (GRCm39) H54L probably benign Het
P3h1 C T 4: 119,092,480 (GRCm39) T171I probably damaging Het
Pcdhb1 A G 18: 37,399,366 (GRCm39) E439G possibly damaging Het
Pik3c3 A T 18: 30,423,578 (GRCm39) K225* probably null Het
Pik3c3 A G 18: 30,426,102 (GRCm39) probably benign Het
Pik3r5 T A 11: 68,377,452 (GRCm39) probably null Het
Pnpt1 A C 11: 29,098,272 (GRCm39) probably benign Het
Ppp2r1b T A 9: 50,789,422 (GRCm39) V495D probably damaging Het
Rbfox3 C A 11: 118,396,440 (GRCm39) probably benign Het
Sec14l2 G A 11: 4,053,966 (GRCm39) P234S possibly damaging Het
Sec16a A C 2: 26,328,915 (GRCm39) D1033E probably benign Het
Septin14 A G 5: 129,763,019 (GRCm39) V357A probably damaging Het
Sf3a3 C T 4: 124,612,136 (GRCm39) T131I possibly damaging Het
Snrpa A T 7: 26,892,395 (GRCm39) M55K probably benign Het
Swt1 G T 1: 151,286,760 (GRCm39) T244N probably benign Het
Tbl1xr1 A G 3: 22,246,238 (GRCm39) T253A probably benign Het
Tst G T 15: 78,283,964 (GRCm39) R288S probably benign Het
Vmn2r60 A G 7: 41,785,910 (GRCm39) I238V probably benign Het
Zbtb14 A G 17: 69,695,184 (GRCm39) K294R probably benign Het
Zfp710 T A 7: 79,730,871 (GRCm39) V16E probably damaging Het
Zfpm2 A G 15: 40,965,320 (GRCm39) T602A probably benign Het
Zfr2 G A 10: 81,087,193 (GRCm39) M850I probably benign Het
Other mutations in Actl11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01081:Actl11 APN 9 107,806,181 (GRCm39) missense possibly damaging 0.49
IGL01396:Actl11 APN 9 107,805,964 (GRCm39) missense possibly damaging 0.71
IGL01623:Actl11 APN 9 107,805,775 (GRCm39) missense probably benign 0.03
IGL01660:Actl11 APN 9 107,806,247 (GRCm39) missense probably benign
IGL01912:Actl11 APN 9 107,806,844 (GRCm39) missense probably damaging 0.98
IGL02002:Actl11 APN 9 107,806,529 (GRCm39) missense probably benign 0.08
IGL02266:Actl11 APN 9 107,808,382 (GRCm39) missense possibly damaging 0.76
IGL02535:Actl11 APN 9 107,807,136 (GRCm39) missense possibly damaging 0.71
IGL02692:Actl11 APN 9 107,806,507 (GRCm39) missense probably benign 0.06
IGL02744:Actl11 APN 9 107,807,061 (GRCm39) missense probably benign 0.04
IGL02864:Actl11 APN 9 107,806,186 (GRCm39) missense probably benign 0.25
IGL03037:Actl11 APN 9 107,807,294 (GRCm39) missense probably damaging 0.99
IGL03085:Actl11 APN 9 107,806,749 (GRCm39) missense probably damaging 0.98
R0167:Actl11 UTSW 9 107,806,969 (GRCm39) missense probably damaging 1.00
R0304:Actl11 UTSW 9 107,806,967 (GRCm39) missense probably damaging 1.00
R0959:Actl11 UTSW 9 107,808,434 (GRCm39) missense probably damaging 1.00
R1499:Actl11 UTSW 9 107,808,682 (GRCm39) missense probably damaging 1.00
R1616:Actl11 UTSW 9 107,809,135 (GRCm39) missense probably benign 0.39
R1694:Actl11 UTSW 9 107,807,207 (GRCm39) missense probably damaging 1.00
R1927:Actl11 UTSW 9 107,806,736 (GRCm39) missense possibly damaging 0.88
R2081:Actl11 UTSW 9 107,807,396 (GRCm39) missense probably benign
R2939:Actl11 UTSW 9 107,808,409 (GRCm39) missense possibly damaging 0.84
R3427:Actl11 UTSW 9 107,806,969 (GRCm39) missense probably damaging 1.00
R4812:Actl11 UTSW 9 107,808,329 (GRCm39) missense probably damaging 0.99
R4843:Actl11 UTSW 9 107,806,691 (GRCm39) missense possibly damaging 0.61
R4972:Actl11 UTSW 9 107,807,155 (GRCm39) missense probably benign 0.07
R4989:Actl11 UTSW 9 107,808,615 (GRCm39) missense probably damaging 1.00
R4996:Actl11 UTSW 9 107,808,934 (GRCm39) missense possibly damaging 0.77
R5320:Actl11 UTSW 9 107,808,203 (GRCm39) missense possibly damaging 0.73
R5546:Actl11 UTSW 9 107,806,832 (GRCm39) missense probably benign 0.00
R5810:Actl11 UTSW 9 107,806,420 (GRCm39) missense probably benign 0.23
R6302:Actl11 UTSW 9 107,806,772 (GRCm39) missense probably benign 0.12
R6412:Actl11 UTSW 9 107,807,116 (GRCm39) missense probably benign 0.01
R6835:Actl11 UTSW 9 107,807,761 (GRCm39) missense probably benign
R6891:Actl11 UTSW 9 107,806,346 (GRCm39) missense probably benign 0.03
R7195:Actl11 UTSW 9 107,806,069 (GRCm39) nonsense probably null
R7212:Actl11 UTSW 9 107,805,856 (GRCm39) missense probably damaging 0.99
R8478:Actl11 UTSW 9 107,805,844 (GRCm39) missense possibly damaging 0.81
R8670:Actl11 UTSW 9 107,805,959 (GRCm39) missense possibly damaging 0.76
R8683:Actl11 UTSW 9 107,806,065 (GRCm39) missense probably benign 0.15
R9114:Actl11 UTSW 9 107,808,509 (GRCm39) missense possibly damaging 0.62
R9233:Actl11 UTSW 9 107,807,900 (GRCm39) missense possibly damaging 0.91
R9280:Actl11 UTSW 9 107,808,573 (GRCm39) missense probably damaging 1.00
R9361:Actl11 UTSW 9 107,805,824 (GRCm39) missense probably damaging 1.00
R9565:Actl11 UTSW 9 107,808,121 (GRCm39) missense possibly damaging 0.92
X0024:Actl11 UTSW 9 107,807,704 (GRCm39) missense probably benign 0.01
Z1176:Actl11 UTSW 9 107,808,899 (GRCm39) missense probably benign 0.20
Posted On 2015-04-16